1,3,5-Tri(9H-carbazol-9-yl)benzene - ≥98%(HPLC) , CAS No.148044-07-9

CAS: 148044-07-9 Cat. No.: T123337 Peso molecular: 573.68 PubChem CID: 22218951

GRADE & PURITY ≥98%(HPLC)

Synonyms

TCP | FT-0686898 | 1,3,5-TRI(9-CARBAZOLYL)BENZENE | 1,3,5-Tri(9H-carbazol-9-yl)benzene | AS-39310 | 1,3,5-tris(carbazol-9-yl)benzene | 9-[3,5-di(carbazol-9-yl)phenyl]carbazole | 1,3,5-Tris(carbazol-9-yl)benzene;1,3,5-Tri(9H-carbazol-9-yl)benzene | A847611

Storage

Room temperature

Shipped In

Normal

Descripción general

This material is an advanced host material for phosphorescent guest-host systems; such as used in Organic Light Emitting Diode devices

Specifications

Sinónimos

TCP | FT-0686898 | 1, 3, 5-TRI(9-CARBAZOLYL)BENZENE | 1, 3, 5-Tri(9H-carbazol-9-yl)benzene | AS-39310 | 1, 3, 5-tris(carbazol-9-yl)benzene | 9-[3, 5-di(carbazol-9-yl)phenyl]carbazole | 1, 3, 5-Tris(carbazol-9-yl)benzene;1, 3, 5-Tri(9H-carbazol-9-yl)benzene | A847611

Especificaciones y pureza

≥98%(HPLC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(HPLC)

Nombres e identificadores

• Pubchem Sid: 488200076
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488200076
• Sonrisas canónicas: C1=CC=C2C(=C1)C3=CC=CC=C3N2C4=CC(=CC(=C4)N5C6=CC=CC=C6C7=CC=CC=C75)N8C9=CC=CC=C9C1=CC=CC=C18
• IUPAC Name: 9-[3,5-di(carbazol-9-yl)phenyl]carbazole
• InChIKey: DVNOWTJCOPZGQA-UHFFFAOYSA-N
• INCHI: 1S/C42H27N3/c1-7-19-37-31(13-1)32-14-2-8-20-38(32)43(37)28-25-29(44-39-21-9-3-15-33(39)34-16-4-10-22-40(34)44)27-30(26-28)45-41-23-11-5-17-35(41)36-18-6-12-24-42(36)45/h1-27H
• Isómeros SMILES: C1=CC=C2C(=C1)C3=CC=CC=C3N2C4=CC(=CC(=C4)N5C6=CC=CC=C6C7=CC=CC=C75)N8C9=CC=CC=C9C1=CC=CC=C18
• WGK Alemania: 3
• PubChem CID: 22218951
• Peso molecular: 573.68
• Reaxy-Rn: 14393963

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Indoles and derivatives
      • Subclass Carbazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Indoles and derivatives
• Subclass: Carbazoles
• Intermediate Tree Nodes: Not available
• Direct Parent: Carbazoles
• Alternative Parents: Phenylpyrroles Indoles Benzene and substituted derivatives Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Carbazole - 1-phenylpyrrole - Indole - Benzenoid - Substituted pyrrole - Monocyclic benzene moiety - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: Soluble in Tetrahydrofuran
• Punto de fusión (°C): 325-330°C
• Peso molecular: 573.700 g/mol
• XLogP3: 11.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 573.22 Da
• Monoisotopic Mass: 573.22 Da
• Topological Polar Surface Area: 14.800 Ų
• Heavy Atom Count: 45
• Formal Charge: 0
• Complexity: 837.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Amirbek Bekeshev, Anton Mostovoy, Andrey Shcherbakov, Arai Zhumabekova, Gulbanu Serikbayeva, Maria Vikulova, Victoria Svitkina.  (2023)  Effect of Phosphorus and Chlorine Containing Plasticizers on the Physicochemical and Mechanical Properties of Epoxy Composites.  Journal of Composites Science,  7  (5): (178).  [PMID:] [10.3390/jcs7050178]

2. Jie Yang, Yandi Tang, Huimei Pan, Wei Ma, Wang Luo, Baiyang Chen, Yinan Bu.  (2022)  Precipitating halides by silver carbonate: A facile pretreatment method to enable total organic halogen analysis in water.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2022.122461]

3. Min Xue, Mufan Cao, Chengyang Xu, Dewei Xiao, Xiaogang Zhang.  (2022)  EQCM Investigation of a Dual-Doped Polymer Electrode for Li-Ion Batteries with Improved Reversible Capacity.  ACS Applied Materials & Interfaces,      [PMID:35622015] [10.1021/acsami.2c06004]

4. Fuyu Song, Yue Kong, Changyou Shao, Yi Cheng, Jie Lu, Yehan Tao, Jian Du, Haisong Wang.  (2021)  Chitosan-based multifunctional flexible hemostatic bio-hydrogel.  Acta Biomaterialia,      [PMID:34610476] [10.1016/j.actbio.2021.09.056]

5. Huanhuan Fan, Guo Qiang Xiang, Yule Wang, Heng Zhang, Keke Ning, Junyue Duan, Lijun He, Xiuming Jiang, Wenjie Zhao.  (2018)  Manganese-doped carbon quantum dots-based fluorescent probe for selective and sensitive sensing of 2,4,6-trinitrophenol via an inner filtering effect.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:30015029] [10.1016/j.saa.2018.07.006]

6. Lingyou Meng, Zhuo Li, Binhong Qu, Peng Li, Jianhui Sun, Yang Qu, Ziqing Zhang, Liqiang Jing.  (2025)  Molecular imprinted Bi4O5Br2 nanosheets for visual ultrasensitive chlorophenols detection by developing a dye-photosensitization sensing system.  WATER RESEARCH,      [PMID:40644845] [10.1016/j.watres.2025.124141]